Assembly of single layers: Three-dimensional assembly of single-layered MoS2 is achieved on a large scale via a solution method. The as-prepared tubular architectures have tunable size and mesopores in the shell, which are desirable for applications. As a example, they exhibit excellent lithium storage properties and are highly active for hydrodesulfurization of thiophene resulting from their structural advantages.

Aluminum-ion batteries (AIBs) are regarded as viable alternatives to lithium-ion technology because of their high volumetric capacity, their low cost, and the rich abundance of aluminum. However, several serious drawbacks of aqueous systems (passive film formation, hydrogen evolution, anode corrosion, etc.) hinder the large-scale application of these systems. Thus, nonaqueous AIBs show incomparable advantages for progress in large-scale electrical energy storage. However, nonaqueous aluminum battery systems are still nascent, and various technical and scientific obstacles to designing AIBs with high capacity and long cycling life have not been resolved until now. Moreover, the aluminum cell is a complex device whose energy density is determined by various parameters, most of which are often ignored, resulting in failure to achieve the maximum performance of the cell. The purpose here is to discuss how to further develop reliable nonaqueous AIBs. First, the current status of nonaqueous AIBs is reviewed based on statistical data from the literature. The influence of parameters on energy density is analyzed, and the current situation and existing problems are summarized. Furthermore, possible solutions and concerns regarding the construction of reliable nonaqueous AIBs are comprehensively discussed. Finally, future research directions and prospects in the aluminum battery field are proposed.

Intermetallic Nix My (M = Ga and Sn) nanocrystals with uniform particle size and controlled composition are successfully synthesized via a solution-based co-reduction strategy. The as-obtained nanocrystals are crystalline and structurally ordered. The active-site isolation and modified electronic structure are responsible for the excellent catalytic performance for alkyne semi-hydrogenation of the as-obtained non-precious catalysts.

A main obstacle in the rational development of heterogeneous catalysts is the difficulty in identifying active sites. Here we show metal/oxide interfacial sites are highly active for the oxidation of benzyl alcohol and other industrially important primary alcohols on a range of metals and oxides combinations. Scanning tunnelling microscopy together with density functional theory calculations on FeO/Pt(111) reveals that benzyl alcohol enriches preferentially at the oxygen-terminated FeO/Pt(111) interface and undergoes readily O-H and C-H dissociations with the aid of interfacial oxygen, which is also validated in the model study of Cu 2 O/Ag(111). We demonstrate that the interfacial effects are independent of metal or oxide sizes and the way by which the interfaces were constructed. It inspires us to inversely support nano-oxides on micro-metals to make the structure more stable against sintering while the number of active sites is not sacrificed. The catalyst lifetime, by taking the inverse design, is thereby significantly prolonged.

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